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The VL3 videolaryngoscope for tracheal intubation in adults: A prospective pilot study.
Pascarella, Giuseppe; Caruso, Stefano; Antinolfi, Vincenzo; Costa, Fabio; Sarubbi, Domenico; Agrò, Felice E.
Afiliação
  • Pascarella G; Department of Anesthesia, Intensive Care and Pain Management, Università Campus Bio-Medico di Roma, via Álvaro del Portillo, Rome, Italy.
  • Caruso S; Department of Anesthesia, Intensive Care and Pain Management, Università Campus Bio-Medico di Roma, via Álvaro del Portillo, Rome, Italy.
  • Antinolfi V; Department of Anesthesia, Intensive Care and Pain Management, Università Campus Bio-Medico di Roma, via Álvaro del Portillo, Rome, Italy.
  • Costa F; Department of Anesthesia, Intensive Care and Pain Management, Università Campus Bio-Medico di Roma, via Álvaro del Portillo, Rome, Italy.
  • Sarubbi D; Department of Anesthesia, Intensive Care and Pain Management, Università Campus Bio-Medico di Roma, via Álvaro del Portillo, Rome, Italy.
  • Agrò FE; Department of Anesthesia, Intensive Care and Pain Management, Università Campus Bio-Medico di Roma, via Álvaro del Portillo, Rome, Italy.
Saudi J Anaesth ; 14(3): 318-322, 2020.
Article em En | MEDLINE | ID: mdl-32934623
BACKGROUND: Videolaryngoscopy (VLS) is recommended by international guidelines for the management of difficult airways. We conducted an observational prospective pilot study to assess the efficacy of the new VL3 videolaryngoscope for routine tracheal intubation (TI) in adults; in terms of success rate, the number of attempts, and maneuver duration, including both normal and difficult airways. METHODS: This prospective observational pilot study comprised a sample of 56 adult patients undergoing elective general anesthesia. For each patient, we performed VLS by VL3 recording the following data: successful TI rate, number of attempts, time of intubation, time to glottis visualization, Cormack-Lehane grade (CL), need for external laryngeal pressure, and presence of post-laryngoscopy side effects. RESULTS: TI was successfully carried out in the totality of patients. In only 4 out of 56 cases, the VL3 offered a CL II. The first attempt intubation was achieved in 48 patients (85.7%). In one case, external laryngeal pressure was needed. No CL III or CL IV were observed. We did not find any significant difference between the predicted difficult airways sample and the rest of the population. CONCLUSION: VL3 videolaryngoscope showed to be an effective and safe device for routine TI, even in those patients with predicted difficult airway. More studies are needed to confirm our findings and verify its efficacy even in other settings.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Saudi J Anaesth Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Saudi J Anaesth Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália